Computational study of urea and its homologue glycinamide : conformations, rotational barriers, and relative interactions with sodium chloride

Conformational behaviors of urea and glycinamide have been investigated using the B3LYP functional with the 6-311+G* and 6-311+G** basis sets. Urea monomers have nonplanar minima at all the levels studied, even in the aqueous phase. In the case of glycinamide, the intramolecular hydrogen bond formed...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 23(2007), 10 vom: 08. Mai, Seite 5406-11
1. Verfasser: Singh, Ajeet (VerfasserIn)
Weitere Verfasser: Chakraborty, Shampa, Ganguly, Bishwajit
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Ions Sodium Chloride 451W47IQ8X glycine amide 4JDT453NWO Urea 8W8T17847W Glycine TE7660XO1C
LEADER 01000naa a22002652 4500
001 NLM169624013
003 DE-627
005 20231223121733.0
007 tu
008 231223s2007 xx ||||| 00| ||eng c
028 5 2 |a pubmed24n0566.xml 
035 |a (DE-627)NLM169624013 
035 |a (NLM)17429985 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Singh, Ajeet  |e verfasserin  |4 aut 
245 1 0 |a Computational study of urea and its homologue glycinamide  |b conformations, rotational barriers, and relative interactions with sodium chloride 
264 1 |c 2007 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 27.06.2007 
500 |a Date Revised 19.11.2015 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Conformational behaviors of urea and glycinamide have been investigated using the B3LYP functional with the 6-311+G* and 6-311+G** basis sets. Urea monomers have nonplanar minima at all the levels studied, even in the aqueous phase. In the case of glycinamide, the intramolecular hydrogen bond formed from the amide to the amine is important for stabilizing the global minimum. Bond rotations and nitrogen inversion barriers for glycinamide conformations have also been reported. The DFT calculated results suggest that urea conformers interact preferentially with the {111} surface of sodium chloride and such interactions can be responsible for the change in the habit of sodium chloride. Glycinamide conformers have a lower affinity toward the {111} surface of sodium chloride in water. The pyramidality of nitrogens in urea conformers does not influence the relative trends of interaction energies with sodium chloride surfaces. The mode of interactions predicted at the LDA/PWC/DND level for urea and glycinamide with sodium chloride for both slab and cluster models shows that the amide functionality (-CONH2) interacts with both Na(+) and Cl(-) ions on the {100} surface; however, the carbonyl oxygen of these additives predominantly interacts with the sodium ions on the {111} surface 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Ions  |2 NLM 
650 7 |a Sodium Chloride  |2 NLM 
650 7 |a 451W47IQ8X  |2 NLM 
650 7 |a glycine amide  |2 NLM 
650 7 |a 4JDT453NWO  |2 NLM 
650 7 |a Urea  |2 NLM 
650 7 |a 8W8T17847W  |2 NLM 
650 7 |a Glycine  |2 NLM 
650 7 |a TE7660XO1C  |2 NLM 
700 1 |a Chakraborty, Shampa  |e verfasserin  |4 aut 
700 1 |a Ganguly, Bishwajit  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1992  |g 23(2007), 10 vom: 08. Mai, Seite 5406-11  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:23  |g year:2007  |g number:10  |g day:08  |g month:05  |g pages:5406-11 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_22 
912 |a GBV_ILN_350 
912 |a GBV_ILN_721 
951 |a AR 
952 |d 23  |j 2007  |e 10  |b 08  |c 05  |h 5406-11